Canonical Allele Identifier: CA379274616
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226789C>T , CM000673.2:g.5226789C>T GRCh38
NC_000011.9:g.5248019C>T , CM000673.1:g.5248019C>T GRCh37
NC_000011.8:g.5204595C>T NCBI36
NG_000007.3:g.70827G>A
NG_059281.1:g.5283G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.103G>A ENSP00000494175.1:p.Val35Ile
ENST00000335295.4:c.103G>A MANE Select ENSP00000333994.3:p.Val35Ile
ENST00000380315.2:c.103G>A ENSP00000369671.2:p.Val35Ile
ENST00000475226.1:n.35G>A
ENST00000485743.1:n.154G>A
ENST00000633227.1:c.87G>A ENSP00000488004.1:p.Trp29Ter
NM_000518.4:c.103G>A NP_000509.1:p.Val35Ile
NM_000518.5:c.103G>A MANE Select NP_000509.1:p.Val35Ile